Medical Device Contract Manufacturers
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Qualified source record · not independently verified
TRKS.co.ltd is listed in FDA device registration data in Shippo-cho Aichi, JP with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
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Ueda Japan Radio Co., Ltd. is listed in FDA device registration data in Ueda-shi Nagano, JP with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Qualified source record · not independently verified
UNISIS CORP is listed in FDA device registration data in Kita-Hiroshima-shi Hokkaid?, JP with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Qualified source record · not independently verified
UNISIS CORP. is listed in FDA device registration data in Koshigaya-shi Saitama, JP with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Qualified source record · not independently verified
VIVATEC CO.,LTD. is listed in FDA device registration data in Sakai-shi ?saka, JP with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Qualified source record · not independently verified
WELLSINO JAPAN LTD. is listed in FDA device registration data in Fukui, JP with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Qualified source record · not independently verified
YAMATO TECHNICAL CO.,LTD. is listed in FDA device registration data in Echizen Fukui, JP with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
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YAMURA ELECTRIC INDUSTRY CO., LTD. is listed in FDA device registration data in KITAKAMI-SHI Iwate, JP with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Qualified source record · not independently verified
YASOJIMA PROCEED CO., LTD. Sendai Factory is listed in FDA device registration data in Tomiya-shi Miyagi, JP with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Qualified source record · not independently verified
YASUI CO., LTD. is listed in FDA device registration data in Higashiusuki-gun Miyazaki, JP with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Qualified source record · not independently verified
Yokowo Co., Ltd is listed in FDA device registration data in Tomioka Gunma, JP with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Qualified source record · not independently verified
Yoshikawa Kasei Co., Ltd. Medical Company Osaka Plant is listed in FDA device registration data in Osaka-shi ?saka, JP with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Profiles identify their evidence level. A qualified source record is not an independently verified supplier, certification, capacity statement or recommendation. How we research suppliers
Japan